Javascript must be enabled to continue!
Nuclear alignment in myotubes requires centrosome proteins recruited by nesprin-1
View through CrossRef
ABSTRACT
Myotubes are syncytial cells generated by fusion of myoblasts. Among the numerous nuclei in myotubes of skeletal muscle fibres, the majority are equidistantly positioned at the periphery, except for clusters of multiple nuclei underneath the motor endplate. The correct positioning of nuclei is thought to be important for muscle function and requires nesprin-1 (also known as SYNE1), a protein of the nuclear envelope. Consistent with this, mice lacking functional nesprin-1 show defective nuclear positioning and present aspects of Emery–Dreifuss muscular dystrophy. In this study, we perform small interfering RNA (siRNA) experiments in C2C12 myoblasts undergoing differentiation, demonstrating that the positioning of nuclei requires PCM-1, a protein of the centrosome that relocalizes to the nuclear envelope at the onset of differentiation in a manner that is dependent on the presence of nesprin-1. PCM-1 itself is required for recruiting proteins of the dynein–dynactin complex and of kinesin motor complexes. This suggests that microtubule motors that are attached to the nuclear envelope support the movement of nuclei along microtubules, to ensure their correct positioning in the myotube.
The Company of Biologists
Title: Nuclear alignment in myotubes requires centrosome proteins recruited by nesprin-1
Description:
ABSTRACT
Myotubes are syncytial cells generated by fusion of myoblasts.
Among the numerous nuclei in myotubes of skeletal muscle fibres, the majority are equidistantly positioned at the periphery, except for clusters of multiple nuclei underneath the motor endplate.
The correct positioning of nuclei is thought to be important for muscle function and requires nesprin-1 (also known as SYNE1), a protein of the nuclear envelope.
Consistent with this, mice lacking functional nesprin-1 show defective nuclear positioning and present aspects of Emery–Dreifuss muscular dystrophy.
In this study, we perform small interfering RNA (siRNA) experiments in C2C12 myoblasts undergoing differentiation, demonstrating that the positioning of nuclei requires PCM-1, a protein of the centrosome that relocalizes to the nuclear envelope at the onset of differentiation in a manner that is dependent on the presence of nesprin-1.
PCM-1 itself is required for recruiting proteins of the dynein–dynactin complex and of kinesin motor complexes.
This suggests that microtubule motors that are attached to the nuclear envelope support the movement of nuclei along microtubules, to ensure their correct positioning in the myotube.
Related Results
Mechanisms of non-centrosomal MTOC formation at the nucleus in muscle cells
Mechanisms of non-centrosomal MTOC formation at the nucleus in muscle cells
Mécanismes non-centrosomaux impliqués dans la formation du centre organisateur des microtubules au noyaux des cellules musculaires
Le juste positionnement du noyau ...
PCID2 influences BRCA1/BARD1 Localization and Centrosome Duplication through its functions in Nuclear Protein and mRNA Export
PCID2 influences BRCA1/BARD1 Localization and Centrosome Duplication through its functions in Nuclear Protein and mRNA Export
Nuclear protein export has an emerging role in the regulation of centrosome duplication, a function that involves interaction of centrosomal proteins with the Crm1 nuclear export f...
Optogenetic induction of contractile ability in immature C2C12 myotubes
Optogenetic induction of contractile ability in immature C2C12 myotubes
AbstractMyoblasts can be differentiated into multinucleated myotubes, which provide a well-established and reproducible muscle cell model for skeletal myogenesis in vitro. However,...
Catalytic growth in a shared enzyme pool ensures robust control of centrosome size
Catalytic growth in a shared enzyme pool ensures robust control of centrosome size
Abstract
Accurate regulation of centrosome size is essential for ensuring error-free cell division, and dysregulation of centrosome size has been linked to various pathologies, inc...
Catalytic growth in a shared enzyme pool ensures robust control of centrosome size
Catalytic growth in a shared enzyme pool ensures robust control of centrosome size
Accurate regulation of centrosome size is essential for ensuring error-free cell division, and dysregulation of centrosome size has been linked to various pathologies, including de...
Spatial and mechanical environments regulate the heterogeneity of myonuclei
Spatial and mechanical environments regulate the heterogeneity of myonuclei
Abstract
Skeletal muscle formation involves tight interactions between muscle cells and associated connective tissue fibroblasts. Every muscle displays the same typ...
Centrosome centering and Decentering by microtubule network rearrangement
Centrosome centering and Decentering by microtubule network rearrangement
AbstractThe centrosome is positioned at the cell center by pushing and pulling forces transmitted by microtubules (MTs). Centrosome decentering is often considered to result from a...
Abstract A43: Centrosome amplification favors survival and impairs ovarian cancer progression
Abstract A43: Centrosome amplification favors survival and impairs ovarian cancer progression
Abstract
Epithelial ovarian cancer (EOC) is the most lethal gynecologic malignancy. The most common subtype of EOC is high-grade serous (HGSOC), which responds at le...

